Kim Eun Joo, Lee Rae Kyong, Suh Jeong Eun, Han Sang Seop, Kim Joon Kyum
Toxicology Research Center, Korea Research Institute of Chemical Technology, Yuseong, Daejeon, Korea.
Arzneimittelforschung. 2003;53(4):272-9. doi: 10.1055/s-0031-1297108.
CKD-602 ((20S)-7-[2-(N-isopropylamino)-ethyl]-camptothecin.HCl, CAS 213819-48-8) is a new class of anticancer drug that belongs to the topoisomerase inhibitors. Its effect on the central nervous system (CNS), general behavior, cardiovascular-respiratory system and the other organ systems were studied. When intravenously administered, CKD-602 up to doses of 5 mg/kg caused an increase of body temperature, increase of respiration rate, decrease of gastrointestinal transport, showed analgesic action and produced antisecretory action in pylorus ligated rats. However, CKD-602 showed no effects on general behavior, motor coordination, spontaneous locomotor activity, hexobarbital sleeping time, convulsion, cardiovascular, smooth muscle and urinary tract system. These findings demonstrate that CKD-602 in doses up to 5 mg/kg has minor effects on the CNS in animals. However, CKD-602 does not exert any general pharmacological effects at the dose of 1 mg/kg except the effects on gastric secretion.
CKD - 602((20S)-7-[2-(N - 异丙基氨基)-乙基]-喜树碱盐酸盐,CAS 213819 - 48 - 8)是一类新型抗癌药物,属于拓扑异构酶抑制剂。研究了其对中枢神经系统(CNS)、一般行为、心血管呼吸系统及其他器官系统的影响。静脉注射时,高达5mg/kg剂量的CKD - 602可导致体温升高、呼吸频率增加、胃肠运输减慢,在幽门结扎大鼠中显示出镇痛作用并产生抗分泌作用。然而,CKD - 602对一般行为、运动协调性、自发运动活性、戊巴比妥睡眠时间、惊厥、心血管、平滑肌和泌尿系统均无影响。这些发现表明,高达5mg/kg剂量的CKD - 602对动物的中枢神经系统有轻微影响。然而,除了对胃分泌的影响外,1mg/kg剂量的CKD - 602不产生任何一般药理作用。